A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290109



Internal ID20499327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38509097..38509097hg38UCSC Ensembl
chr15:38801298..38801298hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762941
Supporting Variants
Samples
Known GenesRASGRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290109
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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